Novel 5-HT3 Receptor Antagonists and Methods of Use

ABSTRACT

The subject invention provides useful and novel 5-HT3 antagonists. The subject invention also provides methods for synthesizing the compounds of invention. The invention also provides methods for the treatment of irritable bowel syndrome and other such conditions.

CROSS-REFERENCE TO RELATED APPLICATION

This application is a continuation of co-pending application U.S. Ser.No. 10/348,669, filed Jan. 21, 2003; which claims the benefit of U.S.Provisional Application Ser. No. 60/350,504, filed Jan. 18, 2002.

BACKGROUND OF INVENTION

Irritable bowel syndrome (IBS) is one of the most commongastrointestinal disorder thought to result from dysregulation ofintestinal motor, sensory and CNS function. In the United States, theestimated prevalence is 15% to 20%, and 75% of patients are women.Despite its prevalence, IBS is poorly understood. It is one of over 20functional gastrointestinal (GI) disorders that are not explained byidentifiable structural or biochemical abnormalities. IBS ischaracterized by persistent or recurrent symptoms of abdominal pain withdiarrhea and/or constipation. IBS is believed to relate to abnormalitiesin motility and/or afferent sensitivity as mediated by the centralnervous system. Patients with IBS have a diminished quality of life anduse significant health care resources.

Treatment for patients diagnosed with IBS has included antidepressantdrugs, tranquilizers and laxatives. Pharmacological intervention indiarrhea-predominant IBS focuses on the reduction of bowel motility,spasms and transit times. Peripherally acting opiod ligands such as thepetidine congeners diphenoxylate and loperamide and the k-opiod agonistfedotozine slow gastrointestinal transit by their effects on thecircular and longitudinal muscle. While these drugs show some effects onintestinal motility, their effects on IBS-related abdominal pain andintestinal relief is generally insufficient.

Alosetron, a selective 5-HT3 receptor antagonist closely related toondansetron in terms of chemistry and pharmacology, is the firstcompound of this type to be developed for irritable bowel syndrome.Alosetron and its uses are described in, for example, U.S. Pat. No.6,284,770, which is incorporated herein by reference. A number ofdifferent 5-HT3 receptor antagonists have been disclosed, for examplethose of group A: indisetron, Ro-93777, YM-114, granisetron, talipexole,azasetron, tropisetron, mirtazapine, ramosetron, ondansetron,lerisetron, alosetron, N-3389, zacopride, cilansetron, E-3620,lintopride, KAE-393, itasetron, mosapride and dolasetron.

In UK Patent No. 2209335 there is disclosed, inter alia, the compound2,3,4,5-tetrahydro-5-methyl-2-[(5-methyl-1H-imidazol4-yl)methyl]-1H-pyrido[4,3-b]indol-1-one,now known as alosetron, and pharmaceutically acceptable salts, solvatesand pharmaceutically acceptable equivalents thereof, in particular itshydrochloride salt. 5-HT3 receptor antagonists are known to be useful inthe treatment of a variety of conditions involving 5-HT3receptor-mediated mechanisms, including in particular emesis.

Ondansetron inhibits emesis by blocking 5-HT3 receptors on vagalafferent nerve terminals in the gastrointestinal mucosa and on terminalson the same vagal nerves in the vomiting system located in the dorsalmedulla of brain stem. Alosetron, in various animal models, can reducethe increase in intestinal fluid secretion and motility triggered byserotonin release. Alosetron increases sensory threshold to balloondistension of the rectum, either by a direct effect on afferent painperception, or via an increase in rectal compliance. In addition, 5-HT3receptor antagonists have been shown to slow colonic transit in man(ondansetron and alosetron). Clinical data for up to 3 months oftreatment indicate that alosetron was orally bioavailable andsignificantly superior to both placebo and the smooth muscle relaxant,mebeverine, in improving perception of visceral pain, spasms anddiarrhea in female diarrhea-predominant IBS.

Alosetron received FDA approval for the treatment of IBS in women withdiarrhea in early 2000. It is the first drug to have proven efficacy forIBS. Alosetron (Lotronex™) was launched in the US, its first market andwas also launched in Puerto Rico for the treatment of women withirritable bowel syndrome who have diarrhea as the predominant symptom.However, in November 2000, Glaxo Wellcome withdrew alosetron from the USmarket, prompted by reports of alosetron-associated ischaemic colitis(n=49; characterized by abdominal cramping and pain) and severeconstipation (n=21). The FDA also received 3 reports of deaths whichwere associated with alosetron.

Alosetron has approximately 60% oral bioavailability and a half-life of1.5 hours. Greater variability was seen in the pharmacokinetic profilein all parameters in females compared with males. Females also had 60%greater drug exposure than males, with mean peak plasma concentration45-100% higher. This is attributed to lower clearance and volume ofdistribution in female population. Similar gender-specific differenceshave been reported for ondansetron. At least 12 metabolites weredetected in urine, which were eliminated from plasma with half-lives ofapproximately 3 hours. 6-Hydroxy-alosetron, which is twice as potent asalosetron was not detected in plasma, however the limit of detection was6-fold higher than the Ki for this metabolite.

The pattern of fecal and urinary elimination of alosetron and itsmetabolites is suggestive of enterohepatic recirculation of6-OH-alosetron, resulting in “prolonged” low level exposure. Inaddition, 6-OH-alosetron glucuronide and a hydroxymethyl metabolite alsohave potent 5-HT3 receptor binding affinity. The pharmacoynamic effectsof these metabolites are unknown. Clearance was predominantly bymetabolism and renal excretion. Mass balance studies with radiolabeleddrug indicate that the concentration of circulating metabolite is atleast 10 fold greater than that of alosetron, yet, two-thirds of thecirculating radioactivity cannot be attributed to alosetron or itsmetabolites. This is due to slower elimination and smaller Vd of themetabolites.

Over 1200 patients with IBS received alosetron for at least 12 weeksduring the Phase II and III clinical trials. Constipation was the mostcommonly reported adverse event, occurring in 28% of those takingalosetron and in 3% of those on placebo. This side effect appears to bedose dependent and constipation occurred more frequently in femalepatients. This gender difference is perhaps related to the increaseddrug exposure level in the female patients.

Thus, it would be particularly desirable to find potent and selective5-HT3 antagonists having comparable pharmacodynamic effect to that ofalosetron, with more predictable metabolism and an improved safetyprofile.

BRIEF SUMMARY

The subject invention provides useful and novel 5-HT3 antagonists andmethods of use. The subject invention also provides methods forsynthesizing the compounds of the subject invention. In a specificembodiment, the subject invention also provides methods for thetreatment of irritable bowel syndrome.

Advantageously, the subject invention provides compounds which arereadily metabolized by the physiological metabolic drug detoxificationsystems. Specifically, in a preferred embodiment, the therapeuticcompounds of the subject invention contain an ester group, which doesnot detract from the ability of these compounds to provide a therapeuticbenefit, but which makes these compounds more susceptible to degradationby hydrolases, particularly serum and/or cytosolic esterases. Thesubject invention further provides methods of treatment comprising theadministration of these compounds to individuals in need of 5-HT3antagonist treatment.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 shows the structures of three 5-HT3 antagonists—alosetron,ondansetran, and granisetron.

FIG. 2 shows sites at which alosetron may be modified according to thesubject invention to create analogs (soft chemistry sites) which haveadvantageous pharmacokinetic properties as described herein.

FIG. 3 shows specific analogs of the subject invention as well as theprimary inactive metabolite after the active compound has been exposedto hydrolytic enzymes.

FIG. 4 shows specific analogs of the subject invention as well as theprimary inactive metabolite after the active compound has been exposedto hydrolytic enzymes.

FIG. 5 shows specific analogs of the subject invention as well as theprimary inactive metabolite after the active compound has been exposedto hydrolytic enzymes.

FIG. 6 shows an example of a synthetic scheme which can be used tosynthesize certain specific analogs of the subject invention.

FIG. 7 shows an example of a synthetic scheme which can be used tosynthesize certain specific analogs of the subject invention.

FIG. 8 shows an example of a synthetic scheme which can be used tosynthesize certain specific analogs of the subject invention.

DETAILED DISCLOSURE

The subject invention provides novel 5-HT3 receptor antagonists. In apreferred embodiment, the 5-HT3 anatgonists of the subject invention canbe deactivated to a primary inactive metabolite by hydrolytic enzymes.

Compounds of the present invention can be advantageously used to treatindividuals in need of treatment with a 5-HT3 receptor antagonist. In apreferred embodiment, the compounds of the subject invention are used totreat patients suffering from gastrointestinal disorders as exemplifiedby irritable bowel syndrome. The compounds of the subject invention areparticularly advantageous due to their predictable pharmacokinetics.

As used herein, the term “individual(s)” refers to a mammal to which isadministered a compound or composition of the present invention. Themammal may be, for example a mouse, rat, pig, horse, rabbit, goat, pig,cow, cat, dog, or human. In a preferred embodiment, the individual is ahuman.

Granisetron and ondansetron are potent 5-HT3 antagonists widely used fortreating emesis induced by chemotherapy (FIG. 1). While ondansetron wasthe first to demonstrate 5-HT3 antagonism activity in the colon, therebyreducing the sensation of pain and transit of content through the colon,alosetron was the first compound of this type to be developed forirritable bowel syndrome.

In a specific embodiment, the present invention provides novel alosetronanalogs that are preferentially metabolized by endogenous hydrolyticenzymes. The novel compounds are bioactive molecules having activity onthe gastrointestinal tract and undergoing deactivation to primaryinactive metabolites by hydrolytic enzymes.

Sites at which alosetron can be modified according to the subjectinvention are shown in FIG. 2. Specific analogs of the subjectinvention, as well as the primary metabolites are shown in FIGS. 3-5.

Adverse drug-drug interactions (DDI), elevation of liver function test(LFT) values, and QT prolongation leading to torsades de pointes (TDP)are three major reasons why drug candidates fail to obtain FDA approval.All these causes are, to some extent, metabolism-based. A drug that hastwo metabolic pathways, one oxidative and one non-oxidative, built intoits structure is highly desirable in the pharmaceutical industry. Analternate, non-oxidative metabolic pathway provides the treated subjectwith an alternative drug detoxification pathway (an escape route) whenone of the oxidative metabolic pathways becomes saturated ornonfunctional. While a dual metabolic pathway is necessary in order toprovide an escape metabolic route, other features are needed to obtaindrugs that are safe regarding DDI, TDP, and LFT elevations.

In addition to having two metabolic pathways, the drug should have arapid metabolic clearance (short metabolic half-life) so that bloodlevels of unbound drug do not rise to dangerous levels in cases of DDIat the protein level. Also, if the metabolic half-life of the drug istoo long, then the CYP450 system again becomes the main eliminationpathway, thus defeating the original purpose of the design. In order toavoid high peak concentrations and rapidly declining blood levels whenadministered, such a drug should also be administered using a deliverysystem that produces constant and controllable blood levels over time.

The compounds of this invention have one or more of the followingcharacteristics or properties:

1. Compounds of the invention are metabolized both by CYP450 and by anon-oxidative metabolic enzyme or system of enzymes;

2. Compounds of the invention have a short (up to four (4) hours)non-oxidative metabolic half-life;

3. Oral bioavailability of the compounds is consistent with oraladministration using standard pharmaceutical oral formulations; however,the compounds, and compositions thereof, can also be administered usingany delivery system that produces constant and controllable blood levelsover time;

4. Compounds according to the invention contain a hydrolysable bond thatcan be cleaved non-oxidatively by hydrolytic enzymes;

5. Compounds of the invention can be made using standard techniques ofsmall-scale and large-scale chemical synthesis;

6. The primary metabolites of compounds of this invention result fromthe non-oxidative metabolism of the compounds;

7. The primary metabolites, regardless of the solubility properties ofthe parent drug, is, or are, soluble in water at physiological pH andhave, as compared to the parent compound, a significantly reducedpharmacological activity;

8. The primary metabolites, regardless of the electrophysiologicalproperties of the parent drug, has, or have, negligible inhibitoryactivity at the IK_(R) (HERG) channel at normal therapeuticconcentration of the parent drug in plasma (e.g., the concentration ofthe metabolite must be at least five times higher than the normaltherapeutic concentration of the parent compound before activity at theIK_(R) channel is observed);

9. Compounds of the invention, as well as the metabolites thereof, donot cause metabolic DDI when co-administered with other drugs;

10. Compounds of the invention, as well as metabolites thereof, do notelevate LFT values when administered alone.

In some embodiments, the subject invention provides compounds that haveany two of the above-identified characteristics or properties. Otherembodiments provide for compounds having at least any three of theabove-identified properties or characteristics. In another embodiment,the compounds, and compositions thereof, have any combination of atleast four of the above-identified characteristics or properties.Another embodiment provides compounds having any combination of five toten of the above-identified characteristics or properties. In apreferred embodiment, the compounds of the invention have all tencharacteristics or properties.

In various embodiments, the primary metabolites of the inventivecompounds, regardless of the electrophysiological properties of theparent drug, has, or have, negligible inhibitory activity at the IK_(R)(HERG) channel at normal therapeutic concentrations of the drug inplasma. Preferably, the concentration of the metabolite must be at leastfive times higher than the normal therapeutic concentration of theparent compound before activity at the IK_(R) channel is observed.Preferably, the concentration of the metabolite must be at least tentimes higher than the normal therapeutic concentration of the parentcompotmd before activity at the IK_(R) channel is observed.

Compounds according to the invention are, primarily, metabolized byendogenous hydrolytic enzymes via hydrolysable bonds engineered intotheir structures. The primary metabolites resulting from this metabolicpathway are water soluble and do not have, or show a reduced incidenceof, DDI when administered with other medications (drugs). Non-limitingexamples of hydrolysable bonds that can be incorporated into compoundsaccording to the invention include amide, ester, carbonate, phosphate,sulfate, urea, urethane, glycoside, and other bonds that can be cleavedby hydrolases.

Additional modifications of the compounds disclosed herein can readilybe made by those skilled in the art. Thus, analogs and salts of theexemplified compounds are within the scope of the subject invention.With a knowledge of the compounds of the subject invention skilledchemists can use known procedures to synthesize these compounds fromavailable substrates. The accompanying figures show certain specificcompounds including those substituted with lower (C₁₋₄) alkyl. Theperson skilled in the art having the benefit of the instant disclosurewould appreciate that other substituents could be made in order toarrive at other compounds having the advantageous biological activity(5-HT3 receptor antagonist) and pharmacokinotic properties.

As used in this application, the term “analogs” refers to compoundswhich are substantially the same as another compound but which may havebeen modified by, for example, adding additional side groups. The term“analogs” as used in this application also may refer to compounds whichare substantially the same as another compound but which have atomic ormolecular substitutions at certain locations in the compound.

Analogs of the exemplified compounds can be readily prepared usingcommonly known, standard reactions. These standard reactions include,but are not limited to, hydrogenation, methylation, acetylation, andacidification reactions. For example, new salts within the scope of theinvention can be made by adding mineral acids, e.g., HCl H₂SO₄, etc., orstrong organic acids, e.g., formic, oxalic, etc., in appropriate amountsto form the acid addition salt of the parent compound or its derivative.Also, synthesis type reactions may be used pursuant to known proceduresto add or modify various groups in the exemplified compounds to produceother compounds within the scope of the invention.

The subject invention further pertains to enantiomerically isolatedcompounds, and compositions comprising the compounds, for 5-HT3antagonism. The isolated enantiomeric forms of the compounds of theinvention are substantially free from one another (i.e., in enantiomericexcess). In other words, the “R” forms of the compounds aresubstantially free from the “S” forms of the compounds and are, thus, inenantiomeric excess of the “S” forms. Conversely, “S” forms of thecompounds are substantially free of “R” forms of the compounds and are,thus, in enantiomeric excess of the “R” forms. In one embodiment of theinvention, the isolated enantiomeric compounds are at least about in 80%enantiomeric excess. In a preferred embodiment, the compounds are in atleast about 90% enantiomeric excess. In a more preferred embodiment, thecompounds are in at least about 95% enantiomeric excess. In an even morepreferred embodiment, the compounds are in at least about 97.5%enantiomeric excess. In a most preferred embodiment, the compounds arein at least 99% enantiomeric excess.

A further aspect of the subject invention pertains to the breakdownproducts which are produced when the therapeutic compounds of thesubject invention are acted upon by hydrolytic enzymes, such asesterases. The presence of these breakdown products in urine or serumcan be used to monitor the rate of clearance of the therapeutic compoundfrom a patient.

The compounds of this invention have therapeutic properties similar tothose of the unmodified parent compounds. Accordingly, dosage rates androutes of administration of the disclosed compounds are similar to thosealready used in the art and known to the skilled artisan (see, forexample, Physicians' Desk Reference. 54^(th) Ed., Medical EconomicsCompany, Montvale, N.J., 2000).

The compounds of the subject invention can be formulated according toknown methods for preparing pharmaceutically useful composition.Formulations are described in detail in a number of sources, which arewell known and readily available to those skilled in the art. Forexample, Remington's Pharmaceutical Science by E. W. Martin describesformulation, which can be used in connection with the subject invention.In general, the compositions of the subject invention are formulatedsuch that an effective amount of the bioactive compound(s) composition.

In accordance with the subject invention, pharmaceutical compositionsare provided which comprise, as an active ingredient, an effectiveamount of one or more of the compounds and one or more non-toxic,pharmaceutically acceptable carriers or diluents. Examples of suchcarriers for use in the invention include ethanol, dimethyl sulfoxide,glycerol, silica, alumina, starch, and equivalent carriers and diluents.Further, acceptable carriers can be either solid or liquid. Solid formpreparations include powders, tablets, pills, capsules, cachets,suppositories and dispersible granules. A solid carrier can be one ormore substances, which may act as diluents, flavoring agents,solubilizers, lubricants, suspending agents, binders, preservatives,tablet disintegrating agents or encapsulating materials.

The disclosed pharmaceutical compositions may be subdivided into unitdoses containing appropriate quantities of the active component. Theunit dosage form can be a packaged preparation, such as packetedtablets, capsules, and powders in paper or plastic containers or invials or ampoules. Also, the unit dosage can be a liquid basedpreparation or formulated to be incorporated into solid food products,chewing gum, or lozenges.

The subject invention further provides methods of synthesizing theunique and advantageous therapeutic compounds of the subject invention.Particularly, methods of producing less toxic therapeutic agentscomprising introducing ester groups into therapeutic agents are taught.The ester linkage may be introduced into the compound at a site which isconvenient in the manufacturing process for the compounds of theinvention. Various exemplary synthetic routes for the preparation of thecompounds of the subject invention are described in FIGS. 6-8.Additionally, the sensitivity of the ester linkage may be manipulated bythe addition of side groups which hinder or promote the hydrolyticactivity of the hydrolases or esterases responsible for cleaving thedrug at the ester locus. Methods of adding such side groups, as well asthe side groups themselves, are well known to the skilled artisan andcan be readily carried out utilizing the guidance provided herein.

All patents, patent applications, provisional applications, andpublications referred to or cited herein are incorporated by referencein their entirety, including all figures and tables, to the extent theyare not inconsistent with the explicit teachings of this specification.

It should be understood that the examples and embodiments describedherein are for illustrative purposes only and that various modificationsor changes in light thereof will be suggested to persons skilled in theart and are to be included within the spirit and purview of thisapplication.

1.-23. (canceled)
 24. A method for preparing a compound of Formula I:

wherein X=N or CH; and R=lower alkyl substituted with OH or NH₂;comprising (a) converting a compound of Formula II:

wherein X and R are as defined above; into a compound of Formula III:

wherein X and R are is as defined above; and (b) removing the nitrogenprotecting group from the compound of Formula III to yield the compoundof Formula I.
 25. A method, according to claim 24, wherein theconversion of the compound of Formula II to the compound of Formula IIIemploys 4-(chloromethyl)-5-methyl-2-trityl-1H-imidazole.
 26. A method,according to claim 24, wherein conversion of the compound of Formula IIto the compound of Formula III employs NaH in THF.
 27. A method,according to claim 24, wherein the removal of the nitrogen protectinggroup employs Pd/C and H₂.
 28. A method for preparing a compound ofFormula IV:

wherein X=N or CH; Y=(CH₂)_(n); n is 0; and R=lower alkyl substitutedwith OH or NH₂; comprising converting a compound of Formula V:

wherein X is as defined above; into a compound of Formula VI:

wherein X and R are is as defined above; and removing the nitrogenprotecting group from the compound of Formula VI to yield the compoundof Formula IV.
 29. A method, according to claim 28, wherein theconversion of the compound of Formula V to the compound of Formula VIemploys 4-(chloromethyl)-2-(methylsulfonyl)-1H-imidazole-5-carboxylateester.
 30. A method, according to claim 28, wherein the conversion ofthe compound of Formula V to the compound of Formula VI employs NaH inTHF.
 31. A method, according to claim 28, wherein the removal of thenitrogen protecting group employs HCl.
 32. A method for preparing acompound of Formula VII:

wherein X=N or CH; and R=lower alkyl substituted with OH or NH₂;comprising converting a compound of Formula VIII:

wherein X and R are as defined above; into a compound of Formula IX:

wherein X and R are is as defined above; and removing the nitrogenprotecting group of the compound of Formula IX to yield the compound ofFormula VII.
 33. A method, according to claim 32, wherein the conversionof the compound of Formula VIII to the compound of Formula IX employs4-(chloromethyl)-5-methyl-2-trityl-1H-imidazole.
 34. A method, accordingto claim 32, wherein the conversion of the compound of Formula VIII tothe compound of Formula IX employs NaH in THF.
 35. A method, accordingto claim 32, wherein the removal of the nitrogen protecting groupemploys Pd/C and H₂.
 36. A method for preparing a compound of Formula I:

wherein X=N or CH; and R=lower alkyl substituted with OH or NH₂;comprising condensing phenylhydrazine with a dione having the formula:

to provide a compound of Formula X:

wherein X is as defined above; converting a compound of Formula X into acompound of Formula XI:

wherein X is as defined above; converting a compound of Formula XI intoa compound of Formula II:

wherein X and R are as defined above; converting a compound of FormulaII into a compound of Formula III:

wherein X and R are is as defined above; and removing the nitrogenprotecting group of the compound of Formula III to yield the compound ofFormula I.
 37. A method, according to claim 36, wherein the conversionof the compound of Formula X to the compound of Formula XI employsAcOH/ZnCl₂.
 38. A method, according to claim 36, wherein the conversionof the compound of Formula XI to the compound of Formula II employs2-bromoacetate ester.
 39. A method, according to claim 36, wherein theconversion of the compound of Formula XI to the compound of Formula IIemploys NaH in THF.
 40. A method, according to claim 36, wherein theconversion of the compound of Formula II to the compound of Formula IIIemploys 4-(chloromethyl)-5-methyl-2-trityl-1H-imidazole.
 41. A method,according to claim 36, wherein the conversion of the compound of FormulaII to the compound of Formula III employs NaH in THF.
 42. A method,according to claim 36, wherein the removal of the nitrogen protectinggroup employs Pd/C and H₂.
 43. A method for preparing a compound ofFormula IV:

wherein X=N or CH; Y=(CH₂)_(n); n is 0; and R=lower alkyl substitutedwith OH or NH₂; comprising condensing 1-methyl-1-phenylhydrazine with adione having the formula:

to provide a compound of Formula XII:

wherein X is as defined above; converting a compound of Formula XII intoa compound of Formula V:

wherein X is as defined above; converting a compound of Formula V into acompound of Formula VI:

wherein X and R are is as defined above; and removing a nitrogenprotecting group of the compound of Formula VI to yield the compound ofFormula IV.
 44. A method, according to claim 43, wherein the conversionof the compound of Formula XII to the compound of Formula V employsAcOH/ZnCl₂.
 45. A method, according to claim 43, wherein the conversionof the compound of Formula V to the compound of Formula VI employs4-(chloromethyl)-2-(methylsulfonyl)-1H-imidazole-5-carboxylate ester.46. A method, according to claim 43, wherein the conversion of thecompound of Formula V to the compound of Formula VI employs NaH in THF.47. A method, according to claim 43, wherein the removal of the nitrogenprotecting group employs HCl.
 48. A method for preparing a compound ofFormula VII:

wherein X=N or CH; and R=lower alkyl substituted with OH or NH₂;comprising condensing a dione having the formula:

with a hydrazine of Formula XII:

to provide a compound of Formula XII:

wherein X and R are as defined above; converting a compound of FormulaXIII into a compound of Formula VIII:

wherein X and R are as defined above; converting a compound of FormulaVIII into a compound of Formula IX:

wherein X and R are is as defined above; and removing the nitrogenprotecting group of the compound of Formula IX to yield the compound ofFormula VII.
 49. A method, according to claim 48, wherein the conversionof the compound of Formula XIII to the compound of Formula VIII employsAcOH/ZnCl₂.
 50. A method, according to claim 48, wherein the conversionof the compound of Formula VIII to the compound of Formula IX employs4-(chloromethyl)-5-methyl-2-trityl-1H-imidazole.
 51. A method, accordingto claim 48, wherein the conversion of the compound of Formula VIII tothe compound of Formula IX employs NaH in THF.
 52. A method, accordingto claim 48, wherein the removal of the nitrogen protecting groupemploys Pd/C and H₂.
 53. A hydrochloride, sulfate, formate, or oxalatesalt of a compound having the following structure:

wherein X=N or CH; Y=(CH₂)_(n); n is 0; and R=lower alkyl optionallysubstituted with OH or NH₂.
 54. A pharmaceutical composition comprisinga salt of claim 53 and at least one pharmaceutically acceptable carrieror diluent.
 55. A method for blocking 5-HT3 activity in a patient inneed of such treatment wherein said method comprises administering tosaid patient a 5-HT3 blocking compound or a pharmaceutically acceptablesalt having the following formula:

a pharmaceutically acceptable salt of a compound having the formula:

a pharmaceutically acceptable salt of a compound having the formula:

wherein X=N or CH; Y=(CH₂)_(n); n is 0; and R=lower alkyl optionallysubstituted with OH or NH₂.
 56. The method, according to claim 55,comprising administering a compound, or a pharmaceutically acceptablesalt of a compound having the following formula:

wherein X=N or CH; and R=lower alkyl substituted with OH or NH₂.
 57. Themethod, according to claim 55, comprising administering apharmaceutically acceptable salt of a compound having the followingformula:

wherein X=N or CH; Y=(CH₂)_(n); n is 0; and R=lower alkyl optionallysubstituted with OH or NH₂.
 58. The method, according to claim 55,comprising administering a pharmaceutically acceptable salt of acompound having the following formula:

wherein X=N or CH; and R=lower alkyl optionally substituted with OH orNH₂.
 59. A method for treating emesis in a patient in need of suchtreatment wherein said method comprises administering to said patient acompound or a pharmaceutically acceptable salt having the followingformula:

wherein X=N or CH; Y=(CH₂)_(n); n is 0; and R=lower alkyl optionallysubstituted with OH or NH₂.
 60. The method, according to claim 59,wherein the patient is human.